Spontaneous Spinal Epidural Hematoma Coexisting Guillan-Barré Syndrome in a Child: A Case Report

Article information

Korean J Spine. 2016;13(3):167-169
Publication date (electronic) : 2016 September 30
doi : https://doi.org/10.14245/kjs.2016.13.3.167
Department of Neurosurgery, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Korea.
Corresponding Author: Geun Sung Song. Department of Neurosurgery, Research Institute for Convergence of Biomedical Science and Technology, Pusan National University School of Medicine, 20 Geumo-ro, Mulgeum-eup, Yangsan 50612, Korea. Tel: +82-55-360-2126, Fax: +82-55-360-2156, gnsong@pusan.ac.kr
Received 2016 April 01; Revised 2016 July 18; Accepted 2016 July 22.


Spontaneous spinal epidural hematoma (SSEH) has been reported as a rare cause of spinal cord compression, especially in children. Clinical features are usually nonspecific, although cervicothoracic location of hematoma could be presented with progressive paraplegia. Guillian-Barré syndrome (GBS) is clinically defined as an acute peripheral neuropathy causing progressive limb weakness. Because SSEH and GBS have very similar signs and symptoms, SSEH could be misdiagnosed as GBS. Nevertheless, they can be presented together. We describe a rare case of SSEH coexisting with GBS.


Spontaneous spinal epidural hematoma (SSEH) is a very rare cause of spinal cord compression, especially in children. Although SSEH has been reported to occur in all age groups, it is most frequent after the fourth or fifth decade16). SSEH is most often defined as a hematoma occurring in the absence of any trauma or iatrogenic procedure3), however, Gopalkrishnan et al.7) suggest that it should be named when hematoma is of idiopathic origin. Clinical presentations of SSEH are miscellaneous and vague, therefore differential diagnosis is important, especially in child. Here, we present the first case of SSEH concomitant with GBS in a child.


A previously healthy 32-month-old male presented to the Emergency Department (ED) with a 1-week history of progressive paraparesis. The patient had a cough and fever for about 2 weeks prior to admission to Pusan National University Yangsan Hospital. Five days before admission, he had difficulty moving his legs spontaneously, 4 days before admission he could not walk without mother's help. On initial evaluation in the ED, the patient was afebrile with normal blood pressure. His neurologic examination was significant for 1/5 strength in his both leg and deep tendon reflexes were absent. Lumbar puncture was performed and cerebrospinal fluid (CSF) examination revealed increased level of protein (544mg/dL) without any other abnormality. Electromyography showed decreased conduction velocity and amplitude on lower limb. Under diagnosis of Guillain-Barré syndrome (GBS), he admitted to the pediatric department and received intravenous immunoglobulin (IVIG) therapy. Strength in his both leg was gradually improved (3/5) after four days of IVIG therapy, but he suddenly started to complain about neck pain. Spinal magnetic resonance image (MRI) demonstrated a dorsal epidural hematoma extending from C4 to T3 level with cord compression (Fig. 1). Conventional spinal angiography was performed to rule out spinal vascular abnormality and it revealed negative finding. His neurologic symptoms were neither improved nor progressed, and the patient was under febrile condition because of bronchopneumonia. Therefore, we decided to perform delayed removal of hematoma. Follow-up spinal MRI with contrast demonstrated enhancement of spinal nerve roots consistent with GBS and there was no significant interval change of the epidural hematoma (Fig. 2). C7 and T1 left hemilaminectomy and drainage of epidural hematoma was performed after 2 weeks of diagnosis of spinal epidural hematoma. Xanthochromic fluid was expelled and thecal sac expansion was identified in the surgical field. The postoperative course was uneventful and the patient regained strength, making a full recovery during 1 week of follow-up.

Fig. 1

Preoperative sagittal (A, B) and axial (C, D) magnetic resonance images showing a dorsal epidural hematoma extending from C4 to T3 level with cord compression.

Fig. 2

Postcontrast sagittal T1-weighted image (A) and axial T1-weighted image (B) demonstrate abnormal enhancement of the nerve root (arrow).


SSEH is a rare surgical emergency, comprising less than 1% of spinal space-occupying lesions18). Since the first case of SSEH was reported by Jackson in 1869, there have been numerous reports of such cases in the literature9). Although SSEH has been reported to occur in all age groups, it is most frequent after the fourth or fifth decade, but is rare in children816).

Clinical presentations of SSEH are usually nonspecific and depend on the involved vertebral level, therefore the diagnosis of SSEH is difficult and differential diagnosis is important. There are several reports of SSEH mimicking meningitis, subarachnoid hemorrhage, GBS and even stroke5101315). Although paraparesis or tetraparesis is a common symptom of cervical SSEH, hemiparesis can also be presented when the hematoma compresses the unilateral corticospinal tract. The SSEH located at the cervicothoracic junction, as in this case, may be presented with progressive paraplegia and neck pain. Cakir et al.5) described a case of SSEH mimicking GBS in a child.

The most common pattern of GBS is the ascending paralysis, weakness beginning in the lower limbs first and migrating towards the trunk, and this is analogous to the symptoms of the SSEH located at the cervicothoracic junction. However, in the present case, there are several evidences of GBS; (1) albuminocytologic dissociation at CSF analysis, (2) decreased conduction velocity and amplitude on electromyography and (3) nerve root enhancement on enhanced spinal MRI. To the best of our knowledge, this is the first case report of SSEH concomitant with GBS.

The diagnosis of GBS is mainly based on clinical features and electrophysiologic and CSF studies. However, there are several reports of that enhanced spinal MR imaging can be used as a supplementary diagnostic modality in the diagnosis of GBS, when the clinical and electrophysiologic findings are equivocal12). The presence of nerve root enhancement on enhanced spinal MRI can be the evidence of GBS, in the present case. Because nerve root generally does not take up much gadolinium on enhanced MRI, nerve root enhancement is thought to be secondary to a breakdown of the blood-nerve barrier.

Although GBS is a potentially life-threatening disease, even with the best treatment available, there are several reports of good prognosis in children, especially1217). Salehiomran et al.17) reported that 16 of 17 patients recovered completely (94.1%). Immediate administration of IVIG after clinical suspicion is recommended, before irreversible nerve damage has taken19).

Even though the pathogenesis of SSEH is remains unclear, 2 main mechanisms of SSEH have been suggested. The bleeding is mostly thought to be venous in origin. The vertebral venous plexus, a valveless low pressure system, is in continuity with the abdominal and thoracic venous system. Lack of valves in the epidural venous plexus makes the area especially vulnerable to any intrinsic change in pressure. The bleeding can occur after activities such as voiding, sneezing, bending, coughing, and coitus. Such activities of normal living can cause fluctuations in the intrathoracic and intra-abdominal pressures, with may cause reversal of blood flow resulting in rupture of a delicate vein in the valveless epidural plexus16). In the present case, repeated cough associated with upper respiratory tract infectio (URI) may be the cause of SSEH result from fluctuations of pressure in abdominal and thoracic venous system, as mentioned previously.

However, Beatty and Winston3) suggest that the origin of SSEH is arterial origin, because the pressure of the epidural venous plexus is lower than the intrathecal pressure, hematomas usually form quickly, and arterial hypertension may sometimes coexist. Some suggest that these arteries are susceptible to abnormal stretching during symmetrical arm movements3).

SSEH can have catastrophic consequences including permanent neurologic deficit and even death, therefore urgent surgical decompression should be considered. Nevertheless, there have been a very few cases in which a good outcome after conservative mannagement4611). Preoperative neurologic deficit and the interval between symptom onset and surgical decompression are believed to be associated with the neurological outcome714). Conservative management and delayed surgical decompression may be justified when there are minimal neurological findings or evidence of an early resolution of neurological deficits, as presented case.


SSEH is rare neurosurgical emergencies and require immediate diagnosis and treatment, because it can cause catastrophic consequences. However, clinical manifestations of the SSEH are nonspecific, so it seems to be misdiagnosed such as GBS, meningitis, and stroke. As seen in this case, SSEH can be concomitant with GBS and performing urgent spinal MRI should be considered when the patient has symptoms like neck pain and meningeal irritation sign.


This work was supported by a 2-Year Research Grant of Pusan National University.


CONFLICT OF INTEREST: No potential conflict of interest relevant to this article was reported.


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Funded by : Pusan National Universityhttp://dx.doi.org/10.13039/501100002543

Fig. 1

Preoperative sagittal (A, B) and axial (C, D) magnetic resonance images showing a dorsal epidural hematoma extending from C4 to T3 level with cord compression.

Fig. 2

Postcontrast sagittal T1-weighted image (A) and axial T1-weighted image (B) demonstrate abnormal enhancement of the nerve root (arrow).